Chrystelle Colas

16PUBLICATIONS

84CO-AUTHORS

Microelectromechanical systems (MEMS)Nutritional epidemiologyCancer geneticsPredictive and prognostic markersMedical infection agents (incl. prions)

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Publications (16)

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|May 18, 2026

<i>MLH1</i> Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation Level.

|May 13, 2026

Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network.

|Feb 13, 2026

Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study.

J Matt McCrary, Els Van Valckenborgh, Denis Horgan

|Jan 29, 2026

Results of a multigene panel testing approach targeting patients with suspected genetic predisposition to pancreatic ductal adenocarcinoma.

Bruno Buecher, Mathilde Warcoin, Emilie Rolland

|Oct 03, 2025

Myeloid neoplasms risks for germline DDX41 pathogenic variants carriers.

Marie-Charlotte Villy, Youenn Drouet, Lise Larcher

|Sep 25, 2025

Hereditary diffuse gastric cancer spectrum associated with germline <i>CTNNA1</i> loss of function revealed by clinical and molecular data from 351 carrier families and over 37 000 non-carrier controls.

Silvana Lobo, Alexandre Dias, Ana Maria Pedro

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Frequent Collaborators

6 joint publications

Dominique Stoppa-Lyonnet

Lisa Golmard

Patrick R Benusiglio

Sophie Nambot

Marie-Charlotte Villy

Mathilde Filser

Marie-Pierre Buisine

Julie Leclerc

Katharina Wimmer

Roseline Vibert

Frequent Collaborators

6 joint publications

Dominique Stoppa-Lyonnet

5 joint publications

Lisa Golmard

3 joint publications

Patrick R Benusiglio

3 joint publications

Sophie Nambot